Neurocysticercosis: diagnosis via metagenomic next-generation sequencing.
APRAXIA
COGNITION
CSF
GAIT
INFECTIOUS DISEASES
Journal
Practical neurology
ISSN: 1474-7766
Titre abrégé: Pract Neurol
Pays: England
ID NLM: 101130961
Informations de publication
Date de publication:
23 Nov 2023
23 Nov 2023
Historique:
accepted:
20
06
2023
medline:
27
11
2023
pubmed:
20
7
2023
entrez:
19
7
2023
Statut:
epublish
Résumé
A 68-year-old Brazilian woman had 3 months of progressive fatigue, difficulty walking and 18 kg weight loss. On examination, there was gait apraxia and executive dysfunction. MR scan of brain showed communicating hydrocephalus and a cerebrospinal fluid showed 105 white cells/µL (≤5), predominantly lymphocytes, protein of 1.35 g/L (0.15-0.45) and the glucose content of 0.06 mmol/L (3.3-4.4). We suspected an infective cause and used of metagenomic next-generation sequencing to diagnose neurocysticercosis. This case highlights the challenge of diagnosing chronic meningitis and the relevance of genetic approaches in diagnosing neurological infections.
Identifiants
pubmed: 37468299
pii: pn-2023-003795
doi: 10.1136/pn-2023-003795
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
509-511Informations de copyright
© Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: None declared.